2. Histopathology and radiology Flashcards

1
Q

What are the 2 broad categorisations of mature bone?

A

Cortical

Cancellous

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2
Q

What % of bone is cortical and where is cortical bone most abundant?

A

80% of bone

Long bones

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3
Q

Describe the structure of cortical bone

A

Mature, lamellar bone - PARALLEL lamellae

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4
Q

Describe the structure of cancellous bone

A

Mature, lamellar bone - CONCENTRIC lamellae

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5
Q

What is the primary function of cancellous bone and where is it most abundant?

A

Metabolic fx - can dissolve/ resorb quickly for Ca++ homeostasis
Vertebrae and pelvis

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6
Q

Describe the process of mineralisation

A

Process through which an organic substance becomes impregnated by inorganic substances

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7
Q

What name is given to immature bone? Describe it structure

A

Woven bone

Irregularly-arranged collagen

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8
Q

What are the cannaliculae in bone?

A

Communication channels for osteocytes

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9
Q

What can be seen where there is osteoclast activity?

A

Howship’s lacunae

= “bite-marks” where breakdown is occuring

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10
Q

Recall the relative proportions of organic and inorganic matter in bone, and summarise the composition of each of these

A

Organic (cells and protein matrix) = 35%

Inorganic (Ca hydroxyapatite) = 65%

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11
Q

What is the role of the RANK ligand in bone homeostasis?

A

When RANK combines with RANK-L osteoclasts are stimulated to differentiate

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12
Q

By what mechanism is osteoclast action inhibited?

A

Osteoprotegerin

Inhibitor of RANK:RANK-L binding

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13
Q

Where are osteocytes located in bone?

A

Lacunae

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14
Q

Distinguish between primary and secondary osteoperosis

A
Primary = age-related, post-menopause
Secondary = caused by drugs (eg thyroid drugs) or systemic disease
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15
Q

Recall the key distinguishing features of osteoperosis from other metabolic bone diseases

A

NORMAL mineralisation so serum biochemistry is normal - just a reduced mass of bone

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16
Q

What is raised ALP indicative of? Give 4 examples of where this might be seen

A

Increased bone turnover

  1. Paget’s
  2. Osteomalacia
  3. Bony Mets
  4. HyperPTHism
17
Q

Sumamrise the possible radiological findings in osteoperosis

A

MAY BE NORMAL
OR
1. Osteopaenic
2. Osteosclerotic

18
Q

Why might osteoperosis demonstrate osteopaenia

A

Loss of bone quantity rather than quality

19
Q

How does osteopaenia appear radiologically?

A

Reduced opacity

20
Q

What is osteosclerosis?

A

Increased bone density

21
Q

Recall 2 key features of osteomalacia radiologically

A
  1. Looser’s zone fractures (horizontal fracture in cortical bone)
  2. Codfish vertebrae
    (biconcave vertebrae)
22
Q

Recall 2 radiological features of Paget’s disease

A
  1. Cortical thickening

2. Coarsening trabeculae

23
Q

Describe how primary and secondary hyperPTHism can be distinguished radiologically?

A

Primary = bone resorption
Secondary = bone resorption AND INCREASED DENSITY
Bone resorption has appearance of erosion, and can lead to “brown tumour”

24
Q

What is renal osteodystrophy?

A
Comprises all the skeletal changes of CKS - a combo of:
OsteoMALACIA
OsteoSCLEROSIS
OsteoPEROSIS
OsteoTITIS FIBROSIS CYSTICA
25
Describe the serum biochemistry of renal osteodystrophy (phosphate, calcium, PTH, pH)
HIGH phosphate LOW calcium HIGH PTH Metabolic acidosis
26
How does sclerosis appear radiologically?
Rugged vertebrae (Jersey spine)
27
Recall 3 radiological features of renal osteodystrophy
Brown tumour Jersey Spine Soft tissue calcification around vessels
28
Recall 2 radiological features of Rickets
Cupped and frayed metaphysis due to increased stress | Widenened unmineralised growth plate